US FDA accepts Bristol Myers Squibb's (BMY) new drug application for Iberdomide in patients with relapsed or refractory multiple Myeloma; target action date of August 17th

Bristol Myers Squibb's new drug application for Iberdomide has been accepted by the FDA, marking a significant potential milestone for the company in the oncology space.

Newsquawk StaffPublished 17 Feb 2026, 15:33 UTCOn the live feed at 15:13 UTC — 3 more headlines followed before this page went public

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15:30

UK DMO to sell GBP 3bln of 4.125% Treasury Gilt in 2033 on the 24th of February, via auction

15:17

Bayer (BAYN GY) to make a USD 10.5bln push to settle roundup cases, according to Bloomberg

15:13

US FDA accepts Bristol Myers Squibb's (BMY) new drug application for Iberdomide in patients with relapsed or refractory multiple Myeloma; target action date of August 17th

15:09

US President Trump to visit Georgia state to spotlight economy and affordability

15:06

Amazon's (AMZN) AWS announces up to USD 100mln in Federal credits to accelerates innovation for national security and scientific mission

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Context

The upcoming target action date of August 17th will be critical, as approval could drive future revenue growth and positively impact stock performance, especially if market expectations shift favorably as a result.

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